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THERMOCOOL SMARTTOUCH BI-DIRECTIONAL NAVIGATION CATHETER

FDA premarket approval P040036/S056 · decided 2016-07-18

Approval details

PMA number
P040036
Supplement
S056
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
THERMOCOOL SMARTTOUCH BI-DIRECTIONAL NAVIGATION CATHETER
Generic name
Cardiac ablation percutaneous catheter
Applicant
Biosense Webster, Inc.
Date received
2016-06-28
Decision date
2016-07-18
Days to decision
20 days
Decision code
OK30
Product code
LPB
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
Use of new equipment, the Output Control System, to inspect connectivity of force and navigation sensor coils, the data on the device EEPROM, and compare EEPROM information as well as physical attributes against the Work Order Packet Requirements.

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510(k) clearances by this applicant

RecordFirmDate
CARTO™ 3 EP Navigation System V8.4 (K252972)Biosense Webster, Inc.2026-02-20
CARTO™ 3 EP Navigation System V9.0 with PIU Plus (K254085)Biosense Webster, Inc.2026-01-18
CARTO™ 3 EP Navigation System V8.1 (K252302)Biosense Webster, Inc.2025-08-22
NUVISION™ Ultrasound Catheter; NUVISION™ NAV Ultrasound Catheter (K241540)Biosense Webster, Inc.2024-06-28
SOUNDSTAR™ CRYSTAL Ultrasound Catheter (K240050)Biosense Webster, Inc.2024-06-12
CARTO™ 3 EP Navigation System Software V8.0 (FG-5400-00, FG-5400-00U) (K231207)Biosense Webster, Inc.2023-09-07
PENTARAY® NAV ECO High Density Mapping Catheter, DECANAV® Mapping Catheter, Webster® CS Catheter with Auto ID, Webster® CS Catheter with EZ Steer Technology, Webster® CS Catheter with EZ Steer Technology with Auto ID (K231312)Biosense Webster, Inc.2023-07-10
CARTO VIZIGO® 8.5F Bi-Directional Guiding Sheath (D-1385-01-S, D-1385-02-S, D-1385-03-S) (K231412)Biosense Webster, Inc.2023-07-10